Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model von Guo, Hui, Wang, Tianyun, Wu, Huidan, Long, Min, Coe, Bradley P, Li, Honghui, Xun, Guanglei, Ou, Jianjun, Chen, Biyuan, Duan, Guiqin, Bai, Ting, Zhao, Ningxia, Shen, Yidong, Li, Yun, Wang, Yazhe, Zhang, Yu, Baker, Carl, Liu, Yanling, Pang, Nan, Huang, Lian, Han, Lin, Jia, Xiangbin, Liu, Cenying, Ni, Hailun, Yang, Xinyi, Xia, Lu, Chen, Jingjing, Shen, Lu, Li, Ying, Zhao, Rongjuan, Zhao, Wenjing, Peng, Jing, Pan, Qian, Long, Zhigao, Su, Wei, Tan, Jieqiong, Du, Xiaogang, Ke, Xiaoyan, Yao, Meiling, Hu, Zhengmao, Zou, Xiaobing, Zhao, Jingping, Bernier, Raphael A, Eichler, Evan E, Xia, Kun

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Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum von Hu, Hao, Wu, Lingqian, Feng, Yong, Pan, Qian, Long, Zhigao, Li, Juan, Dai, Heping, Xia, Kun, Liang, Desheng, Niikawa, Norio, Xia, Jiahui

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A novel splicing mutation in COL1A1 gene caused type I osteogenesis imperfecta in a Chinese family von Peng, Hao, Zhang, Yuhui, Long, Zhigao, Zhao, Ding, Guo, Zhenxin, Xue, Jinjie, Xie, Zhiguo, Xiong, Zhimin, Xu, Xiaojuan, Su, Wei, Wang, Bing, Xia, Kun, Hu, Zhengmao

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Data augmentation using virtual word insertion techniques in text classification tasks von Long, Zhigao, Li, Hong, Shi, Jiawen, Ma, Xin

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Importance-aware contrastive learning via semantically augmented instances for unsupervised sentence embeddings von Ma, Xin, Li, Hong, Shi, Jiawen, Zhang, Yi, Long, Zhigao

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A family with partial duplication/deletion 4p due to a balanced t (4; 15) (p16.2; p11.2) translocation von Wu, Lingqian, Meng, Dahua, Zhou, Zhongmin, Du, Juan, Long, Zhigao, Liang, Desheng

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A ZRS duplication causes syndactyly type IV with tibial hypoplasia von Wu, Lingqian, Liang, Desheng, Niikawa, Norio, Ma, Fen, Sun, Miao, Pan, Qian, Long, Zhigao, Zhou, Zhongmin, Yoshiura, Koh-ichiro, Wang, Hua, Sato, Daisuke, Nishimura, Gen, Dai, Heping, Zhang, Xue, Xia, Jiahui

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A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family von Tang, Beisha, Li, Haiyan, Xia, Kun, Jiang, Hong, Pan, Qian, Shen, Lu, Long, Zhigao, Zhao, Guohua, Cai, Fang

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Phenotypic expansion of the interstitial 16p13.3 duplication: A case report and review of the literature von Li, Zhuo, Liu, Jing, Li, Haoxian, Peng, Ying, Lv, Weigang, Long, Zhigao, Liang, Desheng, Wu, Lingqian

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Pre- and postnatal overgrowth in a patient with proximal 4p deletion von Wu, Lingqian, Long, Zhigao, Liang, Desheng, Harada, Naoki, Pan, Qian, Yoshiura, Koh-ichiro, Xia, Kun, Dai, Heping, Niikawa, Norio, Xia, Jiahui

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A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family von Tian, Qi, Li, Yunping, Kousar, Rizwana, Guo, Hui, Peng, Fenglan, Zheng, Yu, Yang, Xiaohua, Long, Zhigao, Tian, Runyi, Xia, Kun, Lin, Haiying, Pan, Qian

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Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia von Jiang, Hong, Tang, Beisha, Xia, Kun, Hu, Zhengmao, Shen, Lu, Tang, Jianguang, Zhao, Guohua, Zhang, Yuhu, Cai, Fang, Pan, Qian, Long, Zhigao, Wang, Guo, Dai, Heping

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The Combination of Suicide Gene Therapy and Radiation Enhances the Killing of Nasopharyngeal Carcinoma Xenographs von Xia, Jiahui, Xia, Kun, Feng, Yong, Tang, Aifa, Tang, Yaoyun, Wu, Lingqian, Liang, Desheng, Cai, Fang, Pan, Qian, Long, Zhigao, Dai, Heping, Zhang, Yunyi, Zhao, Suping, Chen, Zhuchu

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A novel fusion suicide gene yeast CDglyTK plays a role in radio-gene therapy of nasopharyngeal carcinoma von Xia, Kun, Liang, Desheng, Tang, Aifa, Feng, Yong, Zhang, Junyi, Pan, Qian, Long, Zhigao, Dai, Heping, Cai, Fang, Wu, Lingqian, Zhao, Suping, Chen, Zhuchu, Xia, Jiahui

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Disruption of Contactin 4 in two subjects with autism in Chinese population von Guo, Hui, Xun, Guanglei, Peng, Yu, Xiang, Xinying, Xiong, Zhimin, Zhang, Lusi, He, Yiqun, Xu, Xiaojuan, Liu, Yalan, Lu, Lina, Long, Zhigao, Pan, Qian, Hu, Zhengmao, Zhao, Jingping, Xia, Kun

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A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2 von Liang, Desheng, Wu, Lingqian, Pan, Qian, Harada, Naoki, Long, Zhigao, Xia, Kun, Yoshiura, Koh-ichiro, Dai, Heping, Niikawa, Norio, Cai, Fang, Xia, Jiahui

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Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population von Li, Xiaoping, Hu, Zhengmao, He, Yiqun, Xiong, Zhimin, Long, Zhigao, Peng, Yu, Bu, Fengxiao, Ling, Jie, Xun, Guanglei, Mo, Xiaoyun, Pan, Qian, Zhao, Jingping, Xia, Kun

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Automatic material pumping device of bait injection molding machine von LONG ZHIGAO

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Single-motor stirring screw structure of double-color bait injection molding machine von LONG ZHIGAO

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Identification and characterization of human neuronal voltage-gated calcium channel gamma 3 subunit gene von Xia Jiahui, Zhang Huali, Tang, Dongsheng, Tang Xixiang, Dai Heping, Pan, Qian, Long Zhigao, Liao Xiaodong

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